Cell Technician

Hands‑On cGMP Operations

Focus on execution of cGMP manufacturing activities required to deliver the production plan reliably and compliantly. Essential functions of the job include but not limited to:

• Follow cGMP procedures to support manufacturing execution and automated recipes
• Media preparation & transfers / filtration
• Cell culture sampling, monitoring & transferring
• Harvest operations
• Equipment & process troubleshooting
• Deviation identification, reporting
• cGMP procedure development and optimization
• Requesting, staging, and verifying materials for production activities
• Completing batch documentation and reviewing records for accuracy
• Supporting routine cleanroom operations, equipment sanitization, and environmental monitoring
• Cleaning of the facility
• Collection of samples for environmental monitoring
• Removal of process waste
• Operation of Distributed Computer System (DSC)
• Operation of equipment such as Clean‑in‑Place (CIP), Steam‑in‑Place (SIP) skid, Caustic skid, autoclave, part washer, filter integrity tester, biowelders, etc.

• Evidence of good verbal and written communication.
• Ability to work in a fast‑paced dynamic environment with competing priorities.
• Demonstrated ability to collaborate within and between diverse groups.
• Proactive identification and implementation of continuous improvement opportunities.
• Aptitude for learning moderately complex technical systems.
• Able to receive and incorporate feedback – passion for ongoing professional development a plus.
• Must be able to stand for long periods, up to 8 to 10 hours/day.
• Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently.
• Must be able to work scheduled 40 hours with the ability to work overtime as needed.
• Familiarity with computer‑based systems. Word, Excel, and PowerPoint a must.
• Upstream manufacturing
• Use of single‑use bioreactor systems
• Willing to work any shift.

• At least 1 year of relative experience required.
• High school education or GED required.
• AS/BS/BA in science related field, biopharmaceutical or equivalent technical experience preferred.

Candidates must be flexible to work 7:00am‑3:30pm and/or 3:00‑11:00pm EST shifts starting mid‑August (full production period).

During full production period, candidates must be flexible and able/available to work OT hours if needed, some weekend work, and any holidays that occur during production period.

Potential for extension based on performance, need, and budget.